News tagged with fda
FDA warns of infections tied to Tennessee pharmacy
(AP)—Government health officials are investigating several health problems reported with potentially contaminated medications made by a Tennessee specialty pharmacy.
Diseases, Conditions, Syndromes
May 24, 2013 |
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Evaluating a new way to open clogged arteries
Over the past few decades, scientists have developed many devices that can reopen clogged arteries, including angioplasty balloons and metallic stents. While generally effective, each of these treatments ...
Cardiology
May 21, 2013 |
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FDA has safety concerns on Merck insomnia drug
Federal health regulators say an experimental insomnia drug from Merck can help patients fall asleep, but it also carries worrisome side effects, including daytime drowsiness and suicidal thinking.
Medications
May 20, 2013 |
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US approves radiation-based prostate cancer drug
(AP)—The U.S. Food and Drug Administration has approved a new injectable drug that uses radiation to treat advanced prostate cancer that has spread to the bones.
Cancer
May 15, 2013 |
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New FDA survey to assess doc attitudes on DTC advertising
(HealthDay)—The U.S. Food and Drug Administration plans to conduct a new survey involving 2,000 health care professionals to examine their views on direct-to-consumer (DTC) advertising of prescription medications. ...
Health
May 13, 2013 |
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US government files morning-after pill appeal (Update)
(AP)—The government has filed a last-second appeal that will delay the sale of the morning-after contraceptive pill to girls of any age without a prescription.
Health
May 13, 2013 |
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FDA denies request to block generic painkiller
In a surprise move, federal health regulators have denied a request by Endo Health Solutions to block generic versions of its painkiller Opana ER, which the company argued can be more easily abused than its branded product.
Medications
May 10, 2013 |
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Wrigley takes new caffeinated gum off market
(AP)—A Food and Drug Administration investigation into the safety of caffeine-added foods has prompted Wrigley to take its new caffeinated gum off the market for the time being.
Health
May 09, 2013 |
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Merck says FDA reviewing its ragweed allergy therapy
Drugmaker Merck & Co. says the Food and Drug Administration is reviewing its second application to sell a new type of allergy treatment meant to gradually reduce allergic reactions over time, rather than just relieving sneezing, ...
Medications
May 08, 2013 |
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FDA wants cancer warnings for tanning beds
Indoor tanning beds would carry new warnings about the risk of cancer and be subject to additional regulations, under a proposal unveiled by the Food and Drug Administration.
Health
May 06, 2013 |
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FDA reports Samsca may cause liver damage
(HealthDay)—After reviewing data from recent large clinical trials, the U.S. Food and Drug Administration has determined that Samsca (tolvaptan) should not be used for longer than 30 days and should not ...
Medications
May 02, 2013 |
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Weight loss surgery safe and effective for an expanded group of patients
The LAP-BAND weight loss procedure is safe and effective in an expanded group of patients, not just in people who are morbidly obese. This conclusion is reported in a new study published in the scientific journal Obesity. The fi ...
Overweight and Obesity
May 02, 2013 |
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Two new papers on dabigatran etexilate (Pradaxa) and intracranial hemorrhage
The Journal of Neurosurgery Publishing Group is pleased to announce publication of two new studies on dabigatran etexilate (Pradaxa®) and intracranial hemorrhage: one in the Journal of Neurosurgery and the other in Neur ...
Surgery
May 01, 2013 |
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US: Morning-after pill OK for ages 15 and up (Update)
The U.S. government on Tuesday lowered to 15 the age at which girls can buy the morning-after pill without a prescription and said the emergency contraception no longer has to be kept behind pharmacy counters.
Medications
Apr 30, 2013 |
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Kcentra approved to stop severe bleeding in heart patients
(HealthDay)—Kcentra (prothrombin complex concentrate, human) has been approved by the U.S. Food and Drug Administration to treat severe acute bleeding in adults after administration of the anti-clotting drug warfarin and ...
Medications
Apr 30, 2013 |
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Food and Drug Administration (United States)
The Food and Drug Administration (FDA or USFDA) is an agency of the United States Department of Health and Human Services and is responsible for regulating and supervising the safety of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics. The FDA also enforces section 361 of the Public Health Service Act and the associated regulations, including sanitation requirements on interstate travel as well as specific rules for control of disease on products ranging from pet turtles to semen donations for assisted reproductive medicine techniques.
For more information about Food and Drug Administration (United States), read the full article at
Wikipedia.
This text uses material from Wikipedia and is available under the GNU Free Documentation License.
